FDA 510(k) Applications Submitted by KENNY WALSH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K112381 | 08/17/2011 | HI TORQUE CONNECT GUIDEWIRE | LAKE REGION MEDICAL |
| K212666 | 08/23/2021 | Neuromark System | Neurent Medical |
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